(Received 5 July 1986; accepted 26 August 1986)
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The electron impact mass spectrum of N-ethyl-1-phenylcyclohexylamine (PCE) was studied using both deuterium-labeled compounds and structurally related analogs. The deuterium-labeled compounds used were d2 · PCE with two deuterium atoms on the methylene carbon of the N-ethyl group, d3 · PCE with three deuterium atoms on the methyl carbon of the N-ethyl group, d4 · PCE with four deuterium atoms on the β carbons of the cyclohexyl rings, and d5 · PCE with five deuterium atoms on the phenyl ring. Structurally related compounds used included the N,N-dimethyl, N-propyl, and cyclopentyl analogs. The identities of some major fragments and possible pathways leading to their formation are shown. Electron impact mass spectroscopy is shown to be a definitive test for the identification of PCE.
Forensic chemist, Drug Enforcement Administration, Miami, FL
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